Desert date seed extract-loaded chitosan nanoparticles ameliorate hyperglycemia and insulin deficiency through the reduction in oxidative stress and inflammation

Plants represents a huge source of bioactive materials that have been used since the old times in the treatment of many diseases. Balanites aegyptiaca, known as desert date, has been used in treatment of fever, diabetes and bacterial infection. Desert dates contains a hard seed that resembles 50–60% of the fruit. The seed extract contains many fatty acids, amino acids and other bioactive materials that gives the extract its antioxidant and anti-inflammatory properties. The study aimed to use Balanites seed extract-loaded chitosan nanoparticles (SeEx-C NPs) for the treatment of streptozotocin (STZ)-induced diabetes in male Sprague Dawley rats. Animals were divided into two main divisions (healthy and diabetic rats). Each division contained seven groups (5 rats/group): control untreated group I, SeEx treated group II and group III (10 and 20 mg/kg b.w., respectively), C NPs treated group IV and group V (10 and 20 mg/kg b.w., respectively) and SeEx-C NPs treated group VI and group VII (10 and 20 mg/kg b.w., respectively). The therapeutical effects of SeEx-C NPs were evaluated through biochemical and immunological assessments in rats’ pancreases. The results showed that SeEx-C NPs (10 and 20 mg/kg b.w.) reduced the oxidative stress and inflammation in rats’ pancreases allowing the islets neogenesis. The loading of SeEx on C NPs allowed the delivery of fatty acids (oleic, lauric and myristic acid), amino acids (lysine, leucine, phenylalanine and valine) and minerals to pancreatic beta-cells in a sustainable manner. SeEx-C NPs administration successfully increased insulin secretion, allowed pancreatic islets neogenesis and reduced oxidative stress and inflammation.


Preparation of seed extract
Fresh fruits of Balanites were collected from trees in the Faculty of Agriculture, Cairo University.The tree and fruits were identified by Professor Gehan Safwat (Professor of biotechnology).The voucher specimens were kept in the herbarium of Botany Department, Faculty of Science, Cairo University.All required approvals were obtained for the study, which complied with all relevant regulations.The seed was collected from the fruits and washed with distilled water.The seeds were dried in the oven (40 °C) for one hour, crushed and grinded into fine powder by the aid of an electric grinder (Panasonic, Japan).Seed powder was mixed with ethanol (80%) and stirred for two hours; then left for three days at room temperature.The extract was filtered followed by centrifugation at 1500 rpm for five minutes 16 .The supernatant was concentrated by a rotary evaporator (R-200, MERCK) to obtain crude SeEx.

Characterization of SeEx and SeEx-C NPs
The chemical composition of seed was performed by the official methods of the association of official analytical chemist 17 at the microanalytical center of Cairo University.Thermo Scientific's Trace Gas chromatog-raphy1310-ISQ mass spectrometer (GC-MS) were used to identify the fatty acids components of SeEx and SeEx-C NPs.Inductively Coupled Plasma-mass spectrometry (ICP-MS) analysis was used to identify the different minerals in SeEx.The amino acids composition in SeEx and SeEx-C NPs was determined by a Beckman 120-C amino acid analyzer.

Preparation of SeEx-C NPs
The C solution was prepared by dissolving C in an aqueous solution of acetic acid (1%, v/v) to a final concentration of 2% (w/v).The C solution received an addition of sodium tripolyphosphate (TPP) solution with continuous mixing at room temperature for 1 h until C NPs is formed.SeEx (5 mg/ml) was mixed with TPP solution for the preparation of SeEx-C NPs 18 .The size and form of the produced NPs were determined using the transmission electron microscope (TEM) and scanning electron microscope (SEM), respectively.

Characterization of SeEx-C NPs
The antioxidant activity of the prepared SeEx and SeEx-C NPs were evaluated from the free radical scavenging effect using 1,1-diphenyl-2-picryl hydrazyl (DPPH) according to Farid et al. 18 .Different concentrations of SeEx and SeEx-C NPs were mixed with DPPH solution and allowed to stand for 30 min at room temperature.With ascorbic acid used as a control, the absorbance (abs) was measured at 517 nm and the antioxidant capacity was calculated from the equation: Prothrombin time (PT) and partial thromboplastin time (PTT) were measured to evaluate the anticoagulant activity of SeEx and SeEx-C NPs with the use of heparin as a control 18 .Membrane stabilizing assay, using rats' red blood cells, was used to assess the anti-inflammatory capacity of SeEx and SeEx-C NPs.Different concentrations were mixed with distilled water (hypotonic solution) or saline (isotonic solution); with indomethacin used as a control.The formed mixtures were incubated at 37 °C for 60 min followed by a period of incubation (3 min).The released hemoglobin, in the supernatant, was measured at 540 nm.
The MTT (3-(4,5-dimethylthiazol-2-yl)-2-5-diphenyltetrazolium bromide) assay was used to determine the cytotoxicity of prepared SeEx and SeEx-NPs 18 .Different concentrations were mixed with RPMI culturing media and added to Caco-2 cells monolayers in plates and incubated for 24 h at 37 °C in 5% CO 2 .After incubation, MTT was added to the cultures and the plates were incubated for another 4 h; followed by the addition of DMSO to solubilize formazan.The absorbance was read at 650 nm.

Experimental design
The study was performed according to the international guidelines for the care and use of laboratory animals and in compliance with the ARRIVE guidelines.The study was approved by the ethics committee of October University for Modern Sciences and Arts (MSA 0323).Male Sprague Dawley rats (10 weeks and 170-200 g) were purchased from the National Organization for Drug Control and Research (Egypt) and were divided into two main divisions (healthy and diabetic rats).Each division contained seven groups (5 rats/group) as the following: Group I: control untreated rats, Group II: SeEx (10 mg/kg b.w.) treated rats, Group III: SeEx (20 mg/kg b.w.) treated rats, Group IV: C NPs (10 mg/kg b.w.) treated rats, Group V: C NPs (20 mg/kg b.w.) treated rats, Group VI: SeEx-C NPs (10 mg/kg b.w.) treated rats and Group VII: SeEx-C NPs (20 mg/kg b.w.) treated rats.
Diabetes induction was performed by the intravenous injection of STZ (65 mg/kg b.w.) after 6 h of fasting (water was provided ad libitum through the fasting hours) 19 .Rats were provided with sucrose dissolved in drinking water (10%) on the first day after STZ injection.Fasting blood glucose (FBG) level was monitored for ten days, where, rats with FBG level more than 150 mg/dl were considered diabetic.SeEx, C NPs and SeEx-C NPs were orally administrated via intragastric tube daily to all experimental groups for 8 weeks.At the end of the study, rats were anesthetized with sodium pentobarbital (80 mg/kg b.w.).Blood samples were collected through

Oxidative stress and immunological measurements
The oxidative stress in pancreatic tissue homogenates was assessed by measuring the antioxidant enzymes (CAT, SOD and GSH) by ELISA (MBS726781, MBS036924 and MBS265966; MyBioSource, USA).Lipid peroxidation in pancreas was evaluated through measuring MDA by ELISA (MBS268427, MyBioSource, USA).The effect of STZ administration and the anti-inflammatory effect of tested treatments in rat's pancreas were demonstrated by measuring the pro-inflammatory cytokines (TNF-α, IL-1β, IL-6 and IL-4).

Statistical analysis
Results were examined by one way analysis of variance (ANOVA) and compared with Tukey's homogeneity test.Results were expressed as mean ± standard deviation (SD), and considered significant when P value was less than 0.05.

Ethics approval
All experimental procedures were carried out in accordance with the international guidelines for the care and use laboratory animals, and the study was conducted in accordance with the guide for the care and use of laboratory animals, Eighth edition (2011).The study has been approved by the ethics committee of October University for Modern Sciences and Arts.

Chemical characterization of date seed
According to the proximate analysis, seed contained 6.4% protein, 16.5 crude fibers, 9.8% crude fats, 55.9% carbohydrates.1.3% ash and a 7.6% moisture (Table 1).High levels of potassium and phosphorus (305.4 and 108.5 mg/100 g dry weight, respectively) were found in the date seed; followed by magnesium, calcium and sodium (61.2, 47.5 and 29.8 mg/100 g dry weight).Zinc, iron, manganese and copper were, also, found but with small amount (Table 1).

Characterization of SeEx-C NPs
SEM (Fig. 1A,C) and TEM (Fig. 1B,D) images of both C NPs and SeEx-C NPs showed a smooth spherical NPs with a size range of 63-68 and 81-83 nm, respectively.According to (Fig. 1E,F) the Zeta potential was 25 and − 55 mV for C NPs and SeEx-C NPs, respectively.SeEx-C NPs showed a high antioxidant effect than C NPs and SeEx in a dose dependent manner.This was evident from its high DPPH scavenging effect (Fig. 1G).SeEx-C NPs protected Caco-2 cells at high concentration (up to 250 μg/ml) and achieved high viability % (Fig. 1I); and showed high anti-inflammatory activity where it inhibited red blood cells' hemolysis (Fig. 1J).The anti-coagulant effect of SeEx, C NPs and SeEx-C NPs increased with increasing the tested dose.PT and PTT of SeEx-C NPs were significantly less than those of heparin (Fig. 1H).

Effect of SeEx, C NPs and SeEx-C NPs on body weight and hyperglycemia
Diabetes induction significantly reduced animals' body weight in untreated diabetic GI (200.6 g) when compared to healthy control GI (239.3 g).SeEx and C NPs (either 10 or 20 mg/kg b.w.) administration lead to an enhancement in animals' body weight of treated diabetic GII (210.6),GIII (220.5 g), GIV (211.6 g) and GV (214.9 g), however, animals' body weight remained significantly lower than that of healthy control GI (239.3 g).No significant difference was observed among healthy control GI and SeEx-C NPs treated groups (239.6 and 239.4 g for GVI and GVII).A significant reduction in insulin level and a significant elevation in FBG and FTA levels were noticed after diabetes induction in GI (1.6 ng/ml, 325.1 mg/ml and 307.3 μmol/l, respectively).Only, SeEx-C NPs (either 10 or 20 mg/kg b.w.) have succeeded in decreasing hyperglycemia and increasing insulin level in diabetic treated group.Where, no significant difference was observed in insulin, FBG and FTA levels among healthy control GI and SeEx-C NPs treated groups (Fig. 2).Serum C-peptide level was significantly reduced upon diabetes induction to reach (0.2 ng/ml) in untreated diabetic GI.SeEx administration raised C-peptide level in treated diabetic GII (0.3 ng/ml) and GIII (0.4 ng/ml), but, the levels remained significantly reduced when compared to healthy control GI (0.8 ng/ml).SeEx-C NPs treated diabetic GVI and GVII showed C-peptide levels (0.6 and 0.7, respectively) similar to those of healthy control groups.Figure 3 showed no significant difference in HOMA-IR or QUICKI among the different experimental groups.

Effect of SeEx, C NPs and SeEx-C NPs on oxidative stress
Diabetes induction, in untreated GI, significantly elevated MDA level (17.7 nmol/g tissue) and significantly reduced the antioxidant enzymes levels (35.6 U/g tissue, 33.1 U/g tissue and 59.1 μmol/g tissue for SOD, CAT and GSH, respectively) when compared to those of healthy control GI.SeEx administration (especially 20 mg/kg

Effect of SeEx, C NPs and SeEx-C NPs on pro-inflammatory cytokines
A significant elevation in pro-inflammatory cytokines (119.2, 659.9, 118.2 and 325.6 pg/g tissue for IL-1β, TNF-α, IL-6 and IL-4, respectively) was observed in diabetic control GI when compared to healthy control GI (56.6, 399.9, 69.2 and 215.2 pg/g tissue for IL-1β, TNF-α, IL-6 and IL-4, respectively).SeEx-C NPs showed significant anti-inflammatory effect, in vivo, in diabetic treated GVI and GVII, where, it significantly reduced the pro-inflammatory cytokines levels in those groups to be similar to those of healthy control GI (Fig. 5).On the other hand, SeEx and C NPs administration (either 10 or 20 mg/kg b.w.) were not effective in reducing the inflammation that resulted from diabetes induction by STZ (when compared to SeEx-C NPs).
The pancreatic scoring and morphometric analysis indicated a reduction in islets' size, cellularity and insulin secretion; in addition to, an elevation in beta cell damage, necrosis, inflammatory cells infiltration and edema    in untreated diabetic GI.SeEx-C NPs administration ameliorated these histological alterations indicating islets cells neogenesis and increased insulin secretion Fig. 7.

Discussion
Seeds are a by-product of the manufacture of fruit and are typically handled as litter, fed to animals, or simply thrown away 22 .But seeds, which make up 50-60% of the fresh weight of desert date fruit, are abundant in phytochemical ingredients 23 .Numerous research have been conducted on the pharmacological benefits of date seeds, including their anti-inflammatory, antioxidant, antidiabetic, antimicrobial, and antiviral characteristics 24 .
Date seeds have a significant potential as a dietary therapeutic option for a number of chronic disorders because of their health benefits 25 .Balanites, a member of the Balantiaceae family, is commonly known as desert date according to Anwar and Aastha 26 .It is a wild tree that develops in the desert and savannah parts of Africa 27 .The seed is rich in fatty acids, amino acids, and minerals, that enables the use of the seed extract in many therapeutic approaches (antioxidant, anti-inflammation, antiviral, antimutagenic and antimicrobial).In this study, Balanites seeds were extracted by ethanol (80%) to form crude extract.The seeds were chemically characterized to identify the contained different components that can be loaded on C NPs.The proximate study revealed that the seed has a 6.4% protein content, 16.5% crude fibres, 9.8% crude fats, and 55.9% carbohydrates.The seed included high concentrations of potassium (305.4 mg/100 g dry weight) and phosphorus (108.5 mg/100 g dry weight), which were followed by magnesium, calcium, and sodium (61.2, 47.5, and 29.8 mg/100 g dry weight).In minor amounts, zinc, iron, manganese, and copper were found as well.Alkhoori et al. 28 reported that vitamins found in the seeds included vitamins A, B1 (thiamine), B2 (riboflavin), C, E, K, and folate.They added that seeds contains dietary fibres with functional properties, such as pectin, tannins, lignins, and hemicellulose.Seeds, contained several types of minerals, with K being the most prevalent 29 .Also, Na, Zn, P, F, Se, Ca, Cu, Co, Fe, Mg and B, were found in the seeds 30 .Consuming date seeds is advised for those with hypertension due to their low sodium level.Biglar et al. 31 found that lauric acid, with a content of 18.78-31.61%,and oleic-lauric oil, with a content of 33.38-51.40%,were the two primary fatty acids in date seeds.According to reports, linoleic and palmitic acids are the first two primary fatty acids, with myristic acid coming in third 32 .Our results showed that oleic acid was found in significant concentrations in the fatty acids in SeEx and SeEx-C NPs, followed by lauric and myristic acids.Additionally, significant levels of arachidic acid, capric acid, stearic acid, linoleic acid, palmitic acid, and linoleic acid were found.Other trace amounts of pentadecanoic acid, tridecanoic acid, margaric acid, eicosadienoic acid, and eicosadienoic acid were identified as well.SeEx and SeEx-C NPs were found to contain both of α-and γ-Linolenic acids.
Alkhoori et al. 28 reported that the concentration and type of amino acids in date seeds depended on their maturation stage.According to Niazi et al. 33 , the seed contained high concentration (g/100 g dry seed) of leucine, phenylalanine, and glutamic acid (6.2, 9.8 and16.4g/100 g).Shina et al. 34 reported that the majority of non-essential amino acids were aspartic acid, alanine and tyrosine (1.6, 1.1 and 1.3 g/100 g, respectively).They added that the majority of essential amino acids were leucine, lysine, and phenylalanine (1.6, 1.2 and 1.1 g/100 g, respectively).Our results were in agreement with the previous researches, where, the ratio of non-essential amino acids to essential amino acids was greater.SeEx and SeEx-C NPs contained all nine necessary amino acids.SeEx and SeEx-C NPs has a high quantity of important amino acids, including lysine, leucine, phenylalanine, and valine.The largest concentration of non-essential amino acids was found in glutamic acid, arginine, and aspartic acid followed by alanine, serine, glycine, and proline.
After determination of the bioactive ingredients in SeEx, it was loaded on C NPs to enhance the delivery of these ingredients to the cells.According to our results, SeEx contained several amino and fatty acids, in addition to, several minerals.Some of these compounds have a high molecular weight that render their entry in the cells leading to the loss of their medical benefits.C NPs can decrease the phytonutrients [contained in SeEx) to the nanoscale, enabling them to enter cells with ease 35 .C is a natural polysaccharide that is prepared from chitin, and it is the most utilised and distributed biomaterial after cellulose 36 .The structure of C is identical to cellulose in structure, however C varies greatly from cellulose in that it also includes acetyl amine, hydroxyl and free amino groups 37 .C is safe, biocompatible and biodegradable; and it has been utilised effectively in the medical industry because it's not immunogenic and has a mucoadhesive qualities 38 .The C NPs have been loaded with various plant extracts and polyphenols, and have high antioxidant, anticancer, and anti-inflammatory effects when tested in vitro and/or in vivo 39 .
Both C NPs and SeEx-C NPs were observed under SEM and TEM as smooth spherical NPs with size ranges of 63-68 and 81-83 nm, respectively.The Zeta potential for C NPs and SeEx-C NPs, respectively, was 25 and − 55 mV.In a dose-dependent manner, SeEx-C NPs demonstrated a higher antioxidant impact than C NPs and SeEx.SeEx-C NPs shown excellent anti-inflammatory action by inhibiting the hemolysis of red blood cells while protecting Caco-2 cells at high concentrations (up to 250 μg/ml).With increasing the tested dose, SeEx, C NPs, and SeEx-C NPs showed high anti-coagulant activity.SeEx-C NPs had lower PT and PTT values than heparin.From the characters of prepared SeEx-C NPs, it was clear that NPs can be used safely in in vivo testing.The possibility of treating diabetes, in an induced diabetic rat model, by SeEx-C NPs was examined by monitoring FBG and insulin levels.The antioxidant and anti-inflammatory effects of NPs was evaluated in the pancreatic tissue homogenates.
Our results showed that diabetes induction (in untreated diabetic GI) significantly: 1-reduced animals' body weight, 2-reduced the antioxidant enzymes (SOD, CAT and GSH), 3-elevated MDA level and pro-inflammatory cytokines (IL-1β, TNF-α, IL-6 and IL-4) levels when compared to those of healthy control GI.Moreover, a significant reduction in insulin and C-peptide level; and a significant elevation in FBG and FTA levels was noticed after diabetes induction in GI.SeEx and C NPs (either 10 or 20 mg/kg b.w.) administration lead to an enhancement in animals' body weight, slight reduction in oxidative stress and inflammation in treated diabetic groups.However, SeEx administration (especially 20 mg/kg b.w.) showed better result than C NPs (either 10 or 20 mg/kg b.w.) administration.Only SeEx-C NPs (either 10 or 20 mg/kg b.w.) have succeeded in decreasing hyperglycemia and increasing insulin level in diabetic treated group.No significant difference in HOMA-IR or QUICKI was observed among the different experimental groups, which can be explained by the type of diabetes induced in this experiment.Single high dose of STZ (65 mg/kg b.w.) induces a type of diabetes that is mimic to type I diabetes 40 , which is characterized by a high FBG and low insulin level due to the destructive effect of STZ on pancreatic β-cells.On the other hand, HOMA-IR and QUICKI are indicators of insulin resistance that are calculated from the fasting insulin and glucose levels; and are suitable markers for type II diabetes more than type I diabetes 21 .Moreover, SeEx-C NPs ameliorated the oxidative stress and inflammation that resulted from STZ administration.This was evident from the significant reduction in MDA and pro-inflammatory cytokines; and the significant elevation in the antioxidant enzymes levels.The histological and immunohistochemical examination of pancreas indicated average-sized normocellular islets of Langerhans with marked insulin immunostain in SeEx-C NPs treated diabetic GVI and GVII.On the other hand, untreated diabetic GI showed markedly damaged hypocellular islets of Langerhans with negative insulin immunostain.SeEx-C NPs administration ameliorated these histological alterations indicating islets cells neogenesis and increased insulin secretion (also indicated from increased C-peptide level).
Our results can be explained by the diabetogenic effects of STZ.The plasma membrane's GLUT 2 glucose transporter allows STZ to be accumulated in pancreatic beta-cells.STZ has a methyl nitrosourea moiety that cause DNA alkylation and fragmentation 41 .The damaged DNA then triggers the DNA repair enzyme poly (ADPribose) synthetase leading to ATP and NAD + depletion 42 .Dephosphorylation, which increases the amount of substrates available to xanthine oxidase and causes the production of H 2 O 2 and -OH radicals, serves as a sign of reduced ATP synthesis 43 .Reactive oxygen species (ROS), reactive nitrogen species (RNS), and the development of inflammatory responses are the mechanisms by which STZ causes beta-cells cytotoxicity 44 .SeEx-C NPs administration significantly ameliorated the diabetogenic effects of STZ.This was evident from the biochemical and histopathological results.Where, SeEx-C NPs (10 and 20 mg/kg b.w.) reduced the oxidative stress and inflammation in rats' pancreases allowing the islets neogenesis.
The majority of the plants biologically active compounds such as tannins, flavonoids, and terpenoids are soluble in water but have low absorption rates.Because to their big molecular sizes, insufficient absorption, and inability to pass through lipid membranes, these bioactive components' bioavailability and efficiency are diminished.While herbal medicines have good efficacy in in vitro experiments, in vivo examinations are unable to match their effects.According to Ajazuddin 45 , several essential compounds are seldom used due to their ineffectual qualities or problems combining with other ingredients in the formulation.Numerous nanotechnological techniques have removed this barrier by enabling the use of materials with different properties in the same composition and by potentially changing a substance's actions and properties in an organism 46 .In recent years, several studies have concentrated on using nanotechnology in enhancing the delivery of bioactive components in plant extracts.Ghosh et al. 47 reported that nanotechnology elevated the sustained release of these phytochemicals and decreased the possible side effects of using plant extracts.Alharbi et al. 48used nanotechnology to enhance the topical administration of plants bioactive components.Boosting of the adsorption of green tea and ginseng mixture extract was achieved by using lipid-based structures in the study of Bhattacharya and Ghosh 49 .Also, Gunasekaran et al. 50showed the enhancement of plants bioavailability through nanophytomedicine development.Therefore, the loading of SeEx on C NPs allowed the delivery of fatty acids (oleic, lauric and myristic acid), amino acids (lysine, leucine, phenylalanine, and valine) and minerals to pancreatic beta-cells in a sustainable manner.SeEx-C NPs have the combined antioxidant and anti-inflammatory effects of SeEx and C NPs, which makes these novel NPs a candidate for diabetes therapy.

Conclusion
SeEx-C NPs successfully treated STZ-induced diabetes in male Sprague Dawely rats.It increased insulin secretion, allowed pancreatic islets neogenesis and reduced oxidative stress and inflammation.The study has some limitation such as the small number of experimental animals and examination of only two doses (10 and 20 mg/ kg b.w.).
b.w.) showed better result than C NPs (either 10 or 20 mg/kg b.w.) administration.Only SeEx-C NPs administration significantly ameliorated the oxidative stress that results from STZ administration.Where, no significant difference was observed in MDA, SOD, CAT and GSH levels among healthy control GI and SeEx-C NPs treated groups Fig.4.

Figure 1 .
Figure 1.Shape and size of prepared C NPs and SeEx-C NPs by SEM (A and C) and TEM (B and D), Zeta potential of C NPs (E) and SeEx-C NPs (F), scavenging capacity % (G) (* represented significance (p < 0.05) in comparison to ascorbic acid), clotting time (H) (*represented significance (p < 0.05) in comparison to heparin), viability % (I) (*represented significance (p < 0.05) in comparison to SeEx and #represented significance (p < 0.05) in comparison to C NPs) and hemolysis inhibition % (J) (*represented significance (p < 0.05) in comparison to SeEx and #represented significance (p < 0.05) in comparison to C NPs).

Figure 2 .
Figure 2. Effect of SeEx, C NPs and SeEx-C NPs on body weight (A), FBG (B), insulin (C), FTA (D) and C-peptide (E) levels.Results were expressed as mean ± SD, *represented significance when compared to healthy control (H control GI) and #represented significance when compared to untreated diabetic control (D control GI) (p < 0.05).

Figure 4 .
Figure 4. Effect of SeEx, C NPs and SeEx-C NPs on SOD (A), CAT (B), MDA (C) and GSH (D) levels.Results were expressed as mean ± SD, *represented significance when compared to healthy control (H control GI) and #represented significance when compared to untreated diabetic control (D control GI) (p < 0.05).

Figure 7 .
Figure 7. histopathological pancreatic scoring showing islets' size (A), cellularity (B), beta cells damage (C) and insulin secretion (D); in addition to, morphometric analysis (E).Results were expressed as mean ± SD, *represented significance when compared to healthy control (H control GI) and #represented significance when compared to untreated diabetic control (D control GI) (p < 0.05).

Table 1 .
Proximate analysis and minerals content in date seed.Results were expressed as mean ± standard deviation.

Table 3 .
amino acids composition in SeEx and SeEx-C NPs.Results were expressed as mean ± standard deviation.